The nitro groups on the benzene ring in the reactant serve two purposes. One is to let you know what atoms in the reactant correspond to what atoms in the product. But what role do the nitro groups play electronically – why would the reaction be much slower if these nitro groups weren’t attached to those benzene carbons? Draw any relevant structures to support your answer

what is  the reaction in order to synthesize 1 - propanol from 1-chloropentane

Questions 1015MSC Chemistry of Biological Systems II 186403 1. What is the purpose of the concentrated sulfuric acid in the preparation of aspirin? 2. Anhydride means "without water". Suppose 1 M H₂SO4 were substituted for the concentrated H₂SO4. Would the yield of acetylsalicylic acid be increased, decreased, or unaffected by the substitution? Explain.

A Q2 Provide products. Br₂ AgNO3 H₂0

Hand written solution is not allowed jiger...

help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working

Hello, I do not understand these questions and I am stuck. May I get help please?? Question: Draw the MAJOR organic product(s) for the following reactions. If no reaction occurs state no reaction in the box provided

How would I produce ethoxybenzene from benzene

Which of the following reactions will synthesize phenol from benzene?      1) HNO3 + H2SO4; 2) Fe, HCl; 3) NaNO2, HCl, 0-10 oC; 4) warm H2SO4 and H2O     1) HNO3 + H2SO4; 2) Fe, HCl; 3) NaNO2, HCl, 0-10 oC; 4) CuCN; 5) dilute acid and heat     1) Acetyl chloride & AlCl3; 2) bleach     1) Ph-N2+ + KI; 2) BrMgCH=CH2 in ether, followed by H3O+; 3) warm, conc'd KMnO4     1)  Cl-CH(CH3)-CH2CH2CH3 + FeBr3; 2) hot, conc'd KMnO4

(a) In an acid-catalyzed hydration, one of the following 10 carbon alkynes is expected to produce a single hydration product? Select the correct alkyne and draw the structure of the hydration product that is formed from this alkyne. (I) 2-decyne; (II) 3-decyne; (III) 4-decyne; (IV) 5-decyne; (V) none of these will give a single hydration product. (b) The reaction shown below gives Compound X as the major product. The mass spectrum of X is shown. Br2, H20 Compound X 100 - MS-IW-5644 80 60 40 - 20 - 20 40 60 80 100 120 140 160 180 200 220 m/z Considering the reactions of alkynes and the MS data, de duce which of following structures corresponds to X: Br Br HO, IV V I II II Support your answer with a reaction mechanism for fomation of X and identification of relevant peaks in the mass spectrum. 12 Relative Intensity